A Randomized, Multicenter, Phase II Study of Cetuximab With Docetaxel and Cisplatin as Induction Chemotherapy in Unresectable, Locally Advanced Head and Neck Cancer. (24th August 2015)
- Record Type:
- Journal Article
- Title:
- A Randomized, Multicenter, Phase II Study of Cetuximab With Docetaxel and Cisplatin as Induction Chemotherapy in Unresectable, Locally Advanced Head and Neck Cancer. (24th August 2015)
- Main Title:
- A Randomized, Multicenter, Phase II Study of Cetuximab With Docetaxel and Cisplatin as Induction Chemotherapy in Unresectable, Locally Advanced Head and Neck Cancer
- Authors:
- Lee, Keun-Wook
Koh, Youngil
Kim, Sung-Bae
Shin, Sang-Won
Kang, Jin-Hyoung
Wu, Hong-Gyun
Sung, Myung-Whun
Keam, Bhumsuk
Kim, Dong-Wan
Kim, Tae Min
Kim, Kwang Hyun
Kwon, Tack-Kyun
Hah, J. Hun
Kim, In-Ah
Ahn, Soon-Hyun
Yoon, Dok Hyun
Lee, Sang-Wook
Kim, Sang Yoon
Nam, Soon Yuhl
Jung, Kwang-Yoon
Baek, Seung-Kuk
Hong, Sook Hee
Lee, Se-Hoon
Heo, Dae Seog - Abstract:
- Abstract: Author Summary : Lessons Learned : Addition of cetuximab may affect tolerability and, in turn, affect eventual outcomes. The incidence of prior human papillomavirus infection has emerged as an important variable that can confound trials enrolling patients with oropharyngeal cancer. Background: We investigated the efficacy of cetuximab when added to induction chemotherapy followed by concurrent chemoradiotherapy (CCRT) in patients with locally advanced head and neck squamous cell carcinoma. Methods: Patients were randomized to receive three cycles of docetaxel and cisplatin (TP regimen) with or without cetuximab (TP plus cetuximab [CTP] vs. TP) as induction chemotherapy. Patients in the CTP arm received CCRT with cetuximab and cisplatin, whereas patients in the TP arm received cisplatin alone. The primary endpoint was the objective response rate (ORR) after induction chemotherapy. Results: Overall, 92 patients were enrolled. The ORRs for induction chemotherapy in the CTP and TP arms were not different (81% vs. 82%). Adding cetuximab lowered the completion rate of induction chemotherapy and CCRT and resulted in more frequent dose reductions of the induction chemotherapy, although this did not reach statistical significance. In the CTP and TP arms, respectively, the 3-year progression-free survival (PFS) rates were 70% and 56% ( p = .359), and the overall survival (OS) rates were 88% and 74% ( p = .313). When limited to patients who completed induction chemotherapy,Abstract: Author Summary : Lessons Learned : Addition of cetuximab may affect tolerability and, in turn, affect eventual outcomes. The incidence of prior human papillomavirus infection has emerged as an important variable that can confound trials enrolling patients with oropharyngeal cancer. Background: We investigated the efficacy of cetuximab when added to induction chemotherapy followed by concurrent chemoradiotherapy (CCRT) in patients with locally advanced head and neck squamous cell carcinoma. Methods: Patients were randomized to receive three cycles of docetaxel and cisplatin (TP regimen) with or without cetuximab (TP plus cetuximab [CTP] vs. TP) as induction chemotherapy. Patients in the CTP arm received CCRT with cetuximab and cisplatin, whereas patients in the TP arm received cisplatin alone. The primary endpoint was the objective response rate (ORR) after induction chemotherapy. Results: Overall, 92 patients were enrolled. The ORRs for induction chemotherapy in the CTP and TP arms were not different (81% vs. 82%). Adding cetuximab lowered the completion rate of induction chemotherapy and CCRT and resulted in more frequent dose reductions of the induction chemotherapy, although this did not reach statistical significance. In the CTP and TP arms, respectively, the 3-year progression-free survival (PFS) rates were 70% and 56% ( p = .359), and the overall survival (OS) rates were 88% and 74% ( p = .313). When limited to patients who completed induction chemotherapy, 3-year PFS rates of 78% and 59% ( p = .085) and OS rates of 94% and 73% ( p = .045) were observed in the CTP and TP arms, respectively. Conclusion: Adding cetuximab to sequential treatment did not increase the treatment efficacy and resulted in greater toxicity. In the intent-to-treat population, neither PFS nor OS was improved by the addition of cetuximab to sequential treatment; however, a suggestion of improved survival outcomes was observed in patients completing cetuximab-containing induction chemotherapy. … (more)
- Is Part Of:
- Oncologist. Volume 20:Number 10(2015)
- Journal:
- Oncologist
- Issue:
- Volume 20:Number 10(2015)
- Issue Display:
- Volume 20, Issue 10 (2015)
- Year:
- 2015
- Volume:
- 20
- Issue:
- 10
- Issue Sort Value:
- 2015-0020-0010-0000
- Page Start:
- 1119
- Page End:
- 1120
- Publication Date:
- 2015-08-24
- Subjects:
- Oncology -- Periodicals
Tumors -- Periodicals
Cancérologie -- Périodiques
Tumeurs -- Périodiques
Oncology
Tumors
Neoplasms
Electronic journals
Periodicals
Periodicals
616.994 - Journal URLs:
- https://academic.oup.com/oncolo ↗
https://theoncologist.onlinelibrary.wiley.com/journal/1549490x ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1634/theoncologist.2015-0208 ↗
- Languages:
- English
- ISSNs:
- 1083-7159
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6256.890000
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